Canonical Allele Identifier: PA915980644
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 504644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ile205Thr
CA6197202
NM_001127180.2:c.614T>C