Canonical Allele Identifier: PA915981441
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43241

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu1484Phe
CA132324
NM_001127180.2:c.4450C>T