Canonical Allele Identifier: PA2826462761
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1450187
ClinVar RCV Id: RCV002004786
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val13Gly
CA346729498
NM_001258281.1:c.38T>G