Canonical Allele Identifier: PA658804583
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 505864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys605Arg
CA224836056
NM_000260.4:c.1814A>G