Canonical Allele Identifier: PA658804584
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 517357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg606His
CA6197622
NM_000260.4:c.1817G>A