Canonical Allele Identifier: PA2573181919
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1385015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.His256Arg
CA397687311
NM_001128085.1:c.767A>G