Canonical Allele Identifier: PA099626
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu1858Pro
CA278684
NM_000260.4:c.5573T>C