Canonical Allele Identifier: PA2828319650
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164665
ClinVar RCV Id: RCV000151483 RCV001075256 RCV001109644 RCV001109643 RCV001109642 RCV001514137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg325Cys
CA177368
NM_001369365.1:c.973C>T