Canonical Allele Identifier: PA2825628023
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1525673
ClinVar RCV Id: RCV002036863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp2037Asn
CA381936293
NM_001127180.2:c.6109G>A