Canonical Allele Identifier: PA2825115201
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2188742
ClinVar RCV Id: RCV002620460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gln493Glu
CA381935567
NM_000260.4:c.1477C>G