Canonical Allele Identifier: PA2573180498
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1463810
ClinVar RCV Id: RCV001997799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ser611Asn
CA6197625
NM_001127180.2:c.1832G>A