Canonical Allele Identifier: PA278692
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43298
ClinVar RCV Id: RCV000036203 RCV000675068 RCV001074201 RCV001252670 RCV002513375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu1935Pro
CA278691
NM_000260.4:c.5804T>C