Canonical Allele Identifier: PA916051280
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 178410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Gly132Ser
CA182272
NM_024729.4:c.394G>A