Canonical Allele Identifier: PA915981192
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 179479
ClinVar RCV Id: RCV000156269 RCV000623408 RCV000675162 RCV001004779 RCV001091732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1168Gln
CA184505
NM_001127180.2:c.3503G>A