Canonical Allele Identifier: PA2826634280
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352388
ClinVar RCV Id: RCV002047566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser19Pro
CA346740903
NM_001281494.2:c.55T>C