Canonical Allele Identifier: PA658803355
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 522937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg147Cys
CA6197128
NM_001127180.2:c.439C>T