Canonical Allele Identifier: PA915980551
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306153
ClinVar RCV Id: RCV000298034 RCV000355269 RCV000395630 RCV001059240 RCV001833445
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Thr54Ala
CA6197062
NM_001127180.2:c.160A>G