Canonical Allele Identifier: PA915970522
Gene: TPRN HGNC NCBI

Linked Data

ClinVar Variation Id: 805678
ClinVar RCV Id: RCV000993342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121700.2:p.Leu475Pro
CA375775951
NM_001128228.3:c.1424T>C