Canonical Allele Identifier: PA916010931
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys22Glu
CA16610863
NM_001281492.2:c.64A>G