Canonical Allele Identifier: PA2825440151
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Glu77Ala
CA9592213
NM_001077186.2:c.230A>C