Canonical Allele Identifier: PA2825114868
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1397547
ClinVar RCV Id: RCV001906188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg302Leu
CA6197300
NM_000260.4:c.905G>T