Canonical Allele Identifier: PA915980655
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly214Arg
CA278709
NM_001127180.2:c.640G>A
CA381932112
NM_001127180.2:c.640G>C