Canonical Allele Identifier: PA2825907584
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2900653
ClinVar RCV Id: RCV003737254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Arg88Trp
CA9592217
NM_001145809.2:c.262C>T