Canonical Allele Identifier: PA915981216
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 557219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ser1187Ile
CA381946947
NM_001127180.2:c.3560G>T