Canonical Allele Identifier: PA2826465641
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428459
ClinVar RCV Id: RCV000492018 RCV000691228 RCV003470605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His763Gln
CA46707640
NM_001258281.1:c.2289T>G
CA346730629
NM_001258281.1:c.2289T>A