Canonical Allele Identifier: PA915981053
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 505113
ClinVar RCV Id: RCV000600345 RCV000992402 RCV001834923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg920Leu
CA6197926
NM_001127180.2:c.2759G>T