Canonical Allele Identifier: PA319135
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Pro178Ala
CA319134
NM_000391.4:c.532C>G