Canonical Allele Identifier: PA2825028935
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 929164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Glu129Lys
CA8288909
NM_000049.4:c.385G>A