Canonical Allele Identifier: PA2828321652
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43322
ClinVar RCV Id: RCV000036227 RCV000263244 RCV000320711 RCV000379059 RCV000515066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Val2023Ile
CA132426
NM_001369365.1:c.6067G>A