Canonical Allele Identifier: PA2828319937
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_001356294.1:p.Asp565Asn
CA177374
NM_001369365.1:c.1693G>A