Canonical Allele Identifier: PA182407
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 178477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys268Arg
CA182406
NM_000260.4:c.803A>G