Canonical Allele Identifier: PA2828320062
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg657Cys
CA132231
NM_001369365.1:c.1969C>T