Canonical Allele Identifier: PA915981137
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306182
ClinVar RCV Id: RCV000271790 RCV000302453 RCV000359563 RCV001828314 RCV003298369 RCV001039078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly1139Ser
CA6198059
NM_001127180.2:c.3415G>A