Canonical Allele Identifier: PA091698
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 188888
ClinVar RCV Id: RCV000169243 RCV000489399 RCV000780871
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Gly27Arg
CA274084
NM_000049.4:c.79G>A
CA397681165
NM_000049.4:c.79G>C