Canonical Allele Identifier: PA2829151767
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374610.1:p.Pro370Leu
CA355854751
NM_001387681.1:c.1109C>T