Canonical Allele Identifier: PA915981008
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43183
ClinVar RCV Id: RCV000036087 RCV000286068 RCV000343328 RCV000404583 RCV000904369 RCV001831631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg816His
CA132249
NM_001127180.2:c.2447G>A