Canonical Allele Identifier: PA915981298
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43218
ClinVar RCV Id: RCV000036122 RCV000256123 RCV000504703 RCV000623302 RCV000763279 RCV000984006 RCV001075882 RCV001272514 RCV004528176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1240Gln
CA278657
NM_001127180.2:c.3719G>A