Canonical Allele Identifier: PA2826635713
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 928260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu393Val
CA346750829
NM_001281494.2:c.1177C>G