Canonical Allele Identifier: PA184566
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 179510
ClinVar RCV Id: RCV000156300 RCV001375354 RCV003162638 RCV003335137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Arg1363His
CA184565
NM_001145809.2:c.4088G>A