Canonical Allele Identifier: PA2826465640
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821369
ClinVar RCV Id: RCV001015716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His763Arg
CA346730626
NM_001258281.1:c.2288A>G