Canonical Allele Identifier: PA177373
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu528Arg
CA177372
NM_000260.4:c.1583T>G