Canonical Allele Identifier: PA319172
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Gln158Pro
CA319171
NM_000391.4:c.473A>C