Canonical Allele Identifier: PA645391288
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 408908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Leu398Phe
CA5858705
NM_000391.4:c.1192C>T