Canonical Allele Identifier: PA2826635333
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230514
ClinVar RCV Id: RCV004520665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser309Cys
CA346749550
NM_001281494.2:c.925A>T