Canonical Allele Identifier: PA645413572
Gene: LIPA HGNC NCBI

Linked Data

ClinVar Variation Id: 430634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000226.2:p.Gln298His
CA377516636
NM_000235.4:c.894G>T
CA377516637
NM_000235.4:c.894G>C