Canonical Allele Identifier: PA2825440380
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 637025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Ile284Thr
CA9592426
NM_001077186.2:c.851T>C