Canonical Allele Identifier: PA2826465197
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525696
ClinVar RCV Id: RCV000629899 RCV004002780 RCV002420671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala644Gly
CA034290
NM_001258281.1:c.1931C>G