Canonical Allele Identifier: PA645500005
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 421268
ClinVar RCV Id: RCV000478922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys177Asn
CA16621016
NM_000071.3:c.531G>C
CA410601259
NM_000071.3:c.531G>T