Canonical Allele Identifier: PA2826631998
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 41591
ClinVar Variation Id: 2698505
ClinVar RCV Id: RCV003594839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gln587His
CA010704
NM_001281493.2:c.1761G>T
CA346755231
NM_001281493.2:c.1761G>C