Canonical Allele Identifier: PA129427
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 30739
ClinVar RCV Id: RCV000023718 RCV003228899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Arg941Leu
CA129426
NM_001077186.2:c.2822G>T