Canonical Allele Identifier: PA2826464900
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 628114
ClinVar RCV Id: RCV000772422
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val578_Gln579del
CA913187937
NM_001258281.1:c.1733_1738del