Canonical Allele Identifier: PA2826625271
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser200Pro
CA073692
NM_001281492.2:c.598T>C