Canonical Allele Identifier: PA2826625080
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 822603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser157Asn
CA346740589
NM_001281492.2:c.470G>A