Canonical Allele Identifier: PA915980767
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178667
ClinVar RCV Id: RCV000155424 RCV000594093 RCV000675112 RCV001089675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Tyr403Cys
CA278736
NM_001127180.2:c.1208A>G