Canonical Allele Identifier: PA2573181911
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1478188
ClinVar RCV Id: RCV001998551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Asp234Asn
CA397686119
NM_001128085.1:c.700G>A