Canonical Allele Identifier: PA915980597
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43228
ClinVar RCV Id: RCV000036132 RCV001852746 RCV002482971 RCV003987336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.His133Tyr
CA278660
NM_001127180.2:c.397C>T