Canonical Allele Identifier: PA915981447
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 517448
ClinVar RCV Id: RCV000604476 RCV000679827 RCV001091734 RCV001834957 RCV001291098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp1502Gly
CA6198464
NM_001127180.2:c.4505A>G