Canonical Allele Identifier: PA2826465638
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479858
ClinVar RCV Id: RCV000569186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His763Leu
CA346730628
NM_001258281.1:c.2288A>T