Canonical Allele Identifier: PA2826463051
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91146
ClinVar RCV Id: RCV000076650 RCV001854333 RCV003315405 RCV004019518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys133Arg
CA021524
NM_001258281.1:c.397T>C