Canonical Allele Identifier: PA2826631509
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1021170
ClinVar RCV Id: RCV001320881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu471His
CA346753183
NM_001281493.2:c.1412T>A