Canonical Allele Identifier: PA2828321394
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Leu1809Pro
CA278684
NM_001369365.1:c.5426T>C