Canonical Allele Identifier: PA915968662
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 699687
ClinVar RCV Id: RCV000867593 RCV001502206 RCV002509574
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Lys213Glu
CA8289002
NM_001128085.1:c.637A>G