Canonical Allele Identifier: PA915980601
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.His133Asn
CA177366
NM_001127180.2:c.397C>A