Canonical Allele Identifier: PA2828610959
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362391.1:p.Thr211Ala
CA2751232
NM_001375462.1:c.631A>G