Canonical Allele Identifier: PA2825087530
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile329Thr
CA346741074
NM_000179.3:c.986T>C