Canonical Allele Identifier: PA2825441189
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Glu1484Lys
CA406958778
NM_001077186.2:c.4450G>A