Canonical Allele Identifier: PA136999
Gene: MYO15A HGNC NCBI

Linked Data

ClinVar Variation Id: 45753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057323.3:p.Cys1977Arg
CA136998
NM_016239.4:c.5929T>C