Canonical Allele Identifier: PA2826631200
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 858259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu398Val
CA346750891
NM_001281493.2:c.1192C>G