Canonical Allele Identifier: PA096451
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 212874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gly85Arg
CA319849
NM_000071.3:c.253G>A
CA410602117
NM_000071.3:c.253G>C
CA2579808902
NM_000071.3:c.253_255delinsAGA