Canonical Allele Identifier: PA915980828
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164672
ClinVar RCV Id: RCV000151486 RCV001808415
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu528Arg
CA177372
NM_001127180.2:c.1583T>G