Canonical Allele Identifier: PA2828319769
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 228999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg419Cys
CA6197444
NM_001369365.1:c.1255C>T