Canonical Allele Identifier: PA091687
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 1323943
ClinVar RCV Id: RCV001780648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Asp114Glu
CA397682293
NM_000049.4:c.342C>G
CA397682294
NM_000049.4:c.342C>A