Canonical Allele Identifier: PA915980848
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164674
ClinVar RCV Id: RCV000151488 RCV000666745 RCV001033976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp576Asn
CA177374
NM_001127180.2:c.1726G>A