Canonical Allele Identifier: PA2826049061
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161144.1:p.Thr211Ala
CA2751232
NM_001167672.3:c.631A>G