Canonical Allele Identifier: PA129428
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_001139281.1:p.Arg974Leu
CA129426
NM_001145809.2:c.2921G>T