Canonical Allele Identifier: PA2573165101
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440576
ClinVar RCV Id: RCV001978891
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val642Leu
CA346728676
NM_000251.3:c.1924G>C