Canonical Allele Identifier: PA132329
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43243
ClinVar RCV Id: RCV000036147 RCV001826548 RCV001241478 RCV004018786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Val1491Met
CA132328
NM_000260.4:c.4471G>A