Canonical Allele Identifier: PA2828320633
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 557219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ser1176Ile
CA381946947
NM_001369365.1:c.3527G>T