Canonical Allele Identifier: PA916011162
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89555
ClinVar RCV Id: RCV000075024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser97Ile
CA016239
NM_001281492.2:c.290G>T