Canonical Allele Identifier: PA2826465448
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354604
ClinVar RCV Id: RCV001866507 RCV004009192
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile708Met
CA346729897
NM_001258281.1:c.2124T>G