Canonical Allele Identifier: PA2826635921
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788278
ClinVar RCV Id: RCV002420181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu445Pro
CA346752593
NM_001281494.2:c.1334T>C