Canonical Allele Identifier: PA2827070192
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 3004170
ClinVar RCV Id: RCV003865809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308001.1:p.Ala121Ser
CA410600648
NM_001321072.1:c.361G>T
CA2579813925
NM_001321072.1:c.361_363delinsAGT