Canonical Allele Identifier: PA1139680468
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 866774
ClinVar RCV Id: RCV001075069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg1019Trp
CA224841768
NM_001127180.2:c.3055C>T