Canonical Allele Identifier: PA891847588
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 590160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Thr95Ser
CA5859000
NM_000391.4:c.284C>G
CA379476498
NM_000391.4:c.283A>T