Canonical Allele Identifier: PA645426722
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Val10Ala
CA16616837
NM_000260.4:c.29T>C