Canonical Allele Identifier: PA2826633888
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala1000Thr
CA346761429
NM_001281493.2:c.2998G>A