Canonical Allele Identifier: PA2826133313
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1794424
ClinVar RCV Id: RCV002428728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171480.1:p.Met89Leu
CA410602091
NM_001178009.3:c.265A>T
CA410602093
NM_001178009.3:c.265A>C