Canonical Allele Identifier: PA2826465727
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141396
ClinVar RCV Id: RCV000129900 RCV000236960 RCV000698893 RCV003997534
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu785Val
CA020713
NM_001258281.1:c.2353C>G