Canonical Allele Identifier: PA2826631063
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser366Pro
CA10577271
NM_001281493.2:c.1096T>C