Canonical Allele Identifier: PA2825627914
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43314
ClinVar RCV Id: RCV000036219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Asp1972Gly
CA278703
NM_001127180.2:c.5915A>G