Canonical Allele Identifier: PA2829151089
Gene: LPP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374597.1:p.Ala185Ser
CA355853658
NM_001387668.1:c.553G>T