Canonical Allele Identifier: PA2573180453
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1500753
ClinVar RCV Id: RCV002015891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Tyr298Asn
CA381932917
NM_001127180.2:c.892T>A