Canonical Allele Identifier: PA2573164054
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1313Phe
CA346761495
NM_000179.3:c.3937A>T