Canonical Allele Identifier: PA2826635148
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 628706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe267Ser
CA346748546
NM_001281494.2:c.800T>C