Canonical Allele Identifier: PA182437
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178494
ClinVar RCV Id: RCV000155242 RCV000477766 RCV001241068 RCV001826836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg1832Gln
CA182436
NM_000260.4:c.5495G>A