Canonical Allele Identifier: PA915981372
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 224749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Val1372Gly
CA353603
NM_001127180.2:c.4115T>G