Canonical Allele Identifier: PA118566
Gene: MYO15A HGNC NCBI

Linked Data

ClinVar Variation Id: 6956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057323.3:p.Thr2205Ile
CA118565
NM_016239.4:c.6614C>T