Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA2826132743

Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1744446

ClinVar RCV Id: RCV002342824

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171479.1:p.Ile166Leu	CA410601395 NM_001178008.3:c.496A>C CA2579808532 NM_001178008.3:c.496_498delinsCTT CA2579808533 NM_001178008.3:c.496_498delinsTTG CA2579808534 NM_001178008.3:c.496_498delinsCTG