Canonical Allele Identifier: PA2825115530
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2808815
ClinVar RCV Id: RCV003677168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu618Pro
CA381938403
NM_000260.4:c.1853T>C