Canonical Allele Identifier: PA288995
Gene: PPT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 130022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000301.1:p.Ile134Thr
CA288993
NM_000310.4:c.401T>C