Canonical Allele Identifier: PA658673054
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479858
ClinVar RCV Id: RCV000569186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His829Leu
CA346730628
NM_000251.3:c.2486A>T