Canonical Allele Identifier: PA319213
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207593
ClinVar RCV Id: RCV000189792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Ile468Leu
CA319212
NM_000391.4:c.1402A>C