Canonical Allele Identifier: PA294078
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly289Glu
CA016554
NM_000179.3:c.866_867delinsAA