Canonical Allele Identifier: PA2826625767
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1770363
ClinVar RCV Id: RCV002387711 RCV003759668
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu317Pro
CA346744585
NM_001281492.2:c.950T>C