Canonical Allele Identifier: PA2573183461
Gene: TPRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1348608
ClinVar RCV Id: RCV002044405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121700.2:p.Lys506Arg
CA5362720
NM_001128228.3:c.1517A>G