Canonical Allele Identifier: PA132298
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43214
ClinVar RCV Id: RCV000036118 RCV001196537 RCV001275889 RCV001785454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg120His
CA132297
NM_000260.4:c.359G>A