Canonical Allele Identifier: PA645427089
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg669Gln
CA6197663
NM_000260.4:c.2006G>A