Canonical Allele Identifier: PA132199
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43136
ClinVar RCV Id: RCV000036040 RCV000668099 RCV001762113 RCV001831625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg378His
CA132198
NM_000260.4:c.1133G>A