Canonical Allele Identifier: PA2826626823
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 820658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys562Gln
CA068450
NM_001281492.2:c.1684A>C