Canonical Allele Identifier: PA319170
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Val142Gly
CA319169
NM_000391.4:c.425T>G