Canonical Allele Identifier: PA278733
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178283
ClinVar RCV Id: RCV000155024 RCV000675121 RCV001171535 RCV001850120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ser1276Leu
CA278732
NM_000260.4:c.3827C>T