Canonical Allele Identifier: PA2828320020
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 179146
ClinVar RCV Id: RCV001347350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Cys624Arg
CA183808
NM_001369365.1:c.1870T>C