Canonical Allele Identifier: PA2828320652
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 374511
ClinVar RCV Id: RCV000416022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Cys1190Tyr
CA16043772
NM_001369365.1:c.3569G>A