Canonical Allele Identifier: PA2825907562
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Glu77Ala
CA9592213
NM_001145809.2:c.230A>C