Canonical Allele Identifier: PA2826627160
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu643Phe
CA346753179
NM_001281492.2:c.1927C>T