Canonical Allele Identifier: PA2828321788
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43335
ClinVar RCV Id: RCV000036241 RCV000675126 RCV001275540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly2138Asp
CA278713
NM_001369365.1:c.6413G>A