Canonical Allele Identifier: PA2826632070
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Asp602Glu
CA010773
NM_001281493.2:c.1806T>G
CA346755341
NM_001281493.2:c.1806T>A