Canonical Allele Identifier: PA2741879039
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374605.1:p.Ala22Ser
CA355853658
NM_001387676.1:c.64G>T