Canonical Allele Identifier: PA915983713
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 637025
ClinVar RCV Id: RCV000789010 RCV003317366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Ile284Thr
CA9592426
NM_001145809.2:c.851T>C