Canonical Allele Identifier: PA132289
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43205
ClinVar RCV Id: RCV000036109 RCV000725729 RCV001271745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser1135Tyr
CA132288
NM_000260.4:c.3404C>A