Canonical Allele Identifier: PA2826748467
Gene: LIPA HGNC NCBI

Linked Data

ClinVar Variation Id: 498833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001275908.1:p.Phe112Ser
CA5593637
NM_001288979.2:c.335T>C