Canonical Allele Identifier: PA2826626309
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg447Ser
CA346748747
NM_001281492.2:c.1339C>A