Canonical Allele Identifier: PA2826465656
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90986
ClinVar RCV Id: RCV000076488 RCV000131725 RCV000679306 RCV000659884 RCV001084815
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala768Thr
CA020643
NM_001258281.1:c.2302G>A