Canonical Allele Identifier: PA915980949
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306172
ClinVar RCV Id: RCV000311742 RCV000350852 RCV000406123 RCV001503720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly703Arg
CA6197708
NM_001127180.2:c.2107G>A
CA381939621
NM_001127180.2:c.2107G>C