Canonical Allele Identifier: PA2579798141
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 936814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ala288Ser
CA321091499
NM_000071.3:c.862G>T
CA2579812911
NM_000071.3:c.862_864delinsAGT
CA2579812912
NM_000071.3:c.862_864delinsTCT