Canonical Allele Identifier: PA2826631020
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys358Gln
CA16610909
NM_001281493.2:c.1072A>C