Canonical Allele Identifier: PA658680802
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr672Ile
CA346750694
NM_000179.3:c.2015C>T