Canonical Allele Identifier: PA645500457
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 263326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Arg491His
CA10587936
NM_000071.3:c.1472G>A
CA2579811902
NM_000071.3:c.1472_1473delinsAT