Canonical Allele Identifier: PA2826466032
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237393
ClinVar RCV Id: RCV000565937 RCV000663160 RCV000485086 RCV000231382 RCV000781561
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile860Asn
CA037530
NM_001258281.1:c.2579T>A