Canonical Allele Identifier: PA2825114537
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1045681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg120Cys
CA6197111
NM_000260.4:c.358C>T