Canonical Allele Identifier: PA182273
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 178410
ClinVar RCV Id: RCV000155158 RCV001129343 RCV001550537 RCV003945233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Gly132Ser
CA182272
NM_001145809.2:c.394G>A