Canonical Allele Identifier: PA2825091716
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 925470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu1177Ile
CA346760226
NM_000179.3:c.3529C>A