Canonical Allele Identifier: PA287292
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp904Glu
CA010773
NM_000179.3:c.2712T>G
CA346755341
NM_000179.3:c.2712T>A