Canonical Allele Identifier: PA915980926
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg669Gln
CA6197663
NM_001127180.2:c.2006G>A