Canonical Allele Identifier: PA915981262
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 374511
ClinVar RCV Id: RCV000416022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Cys1201Tyr
CA16043772
NM_001127180.2:c.3602G>A