Canonical Allele Identifier: PA915980507
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 802700
ClinVar RCV Id: RCV000988597 RCV001261014 RCV001036437 RCV001827128
ClinVar Variation Id: 1916542
ClinVar RCV Id: RCV002590506 RCV004065665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly7Arg
CA6197006
NM_001127180.2:c.19G>A
CA381947459
NM_001127180.2:c.19G>C