Canonical Allele Identifier: PA2826626855
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 858259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu570Val
CA346750891
NM_001281492.2:c.1708C>G