Canonical Allele Identifier: PA915980894
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg649Trp
CA6197652
NM_001127180.2:c.1945C>T