Canonical Allele Identifier: PA915980657
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 29924
ClinVar RCV Id: RCV000022815 RCV000215956 RCV000822163 RCV001275897 RCV002251923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp218Asn
CA259686
NM_001127180.2:c.652G>A