Canonical Allele Identifier: PA2825627651
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu1820Pro
CA278684
NM_001127180.2:c.5459T>C