Canonical Allele Identifier: PA645467477
Gene: TSPEAR HGNC NCBI

Linked Data

ClinVar Variation Id: 227135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659428.2:p.Asp639Asn
CA10056257
NM_144991.3:c.1915G>A