Canonical Allele Identifier: PA2825087318
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765963
ClinVar RCV Id: RCV002378792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr305Ile
CA346740728
NM_000179.3:c.914C>T