Canonical Allele Identifier: PA2826465407
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182578
ClinVar RCV Id: RCV000160609 RCV000218725 RCV000456427 RCV003453268
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala697Val
CA020406
NM_001258281.1:c.2090C>T