Canonical Allele Identifier: PA2828319424
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1715116
ClinVar RCV Id: RCV002299401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ile116Val
CA381931416
NM_001369365.1:c.346A>G