Allele Registry

Canonical Allele Identifier: PA1139677459

Gene: MYO7A HGNC NCBI

ClinVar Variation Id: 932085

HGVS (amino-acid)	Matching Registered Transcripts
NP_000251.3:p.Met1994Ile	CA381934246 NM_000260.4:c.5982G>A CA381934248 NM_000260.4:c.5982G>C CA381934250 NM_000260.4:c.5982G>T