Canonical Allele Identifier: PA2826462804
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232406
ClinVar RCV Id: RCV000215101 RCV000227027 RCV001030705 RCV001532987 RCV003997972
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val23Ala
CA10577929
NM_001258281.1:c.68T>C