Canonical Allele Identifier: PA2826629177
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2128264
ClinVar RCV Id: RCV003057495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1175Ile
CA346761444
NM_001281492.2:c.3523C>A