Canonical Allele Identifier: PA915981292
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306183

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Pro1221Arg
CA6198162
NM_001127180.2:c.3662C>G