Canonical Allele Identifier: PA132244
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu765Met
CA132243
NM_000260.4:c.2293C>A