Canonical Allele Identifier: PA278620
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43133
ClinVar RCV Id: RCV000036037 RCV000666645 RCV001268216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu366Pro
CA278619
NM_000260.4:c.1097T>C