Canonical Allele Identifier: PA915980695
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306163
ClinVar RCV Id: RCV000271212 RCV000326285 RCV000365761 RCV001243912
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg292Trp
CA6197289
NM_001127180.2:c.874C>T