Canonical Allele Identifier: PA2829151784
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374611.1:p.Thr211Ala
CA2751232
NM_001387682.1:c.631A>G