Canonical Allele Identifier: PA915980607
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ile134Asn
CA278663
NM_001127180.2:c.401T>A