Canonical Allele Identifier: PA319207
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Thr427Met
CA319206
NM_000391.4:c.1280C>T