Canonical Allele Identifier: PA2580151209
Gene: TPRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2071144
ClinVar RCV Id: RCV002949226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121700.2:p.Leu482_Pro487del
CA5362732
NM_001128228.3:c.1443_1460del