Canonical Allele Identifier: PA278721
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164664
ClinVar RCV Id: RCV000151482 RCV000498129 RCV001291467 RCV001252672 RCV004528877 RCV001810427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu326Gln
CA278720
NM_000260.4:c.977T>A