Canonical Allele Identifier: PA2580151205
Gene: TPRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2347271
ClinVar RCV Id: RCV002963529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121700.2:p.Pro421His
CA5362782
NM_001128228.3:c.1262C>A