Canonical Allele Identifier: PA2829151439
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374603.1:p.Thr211Ala
CA2751232
NM_001387674.1:c.631A>G