Canonical Allele Identifier: PA915981302
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 418368
ClinVar RCV Id: RCV000482515 RCV000504890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Pro1243Leu
CA6198178
NM_001127180.2:c.3728C>T