Canonical Allele Identifier: PA915980939
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 505082
ClinVar RCV Id: RCV000607306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Glu680Gly
CA381939402
NM_001127180.2:c.2039A>G