Canonical Allele Identifier: PA2580136680
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2439252
ClinVar RCV Id: RCV003141587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121557.1:p.Phe135Leu
CA397682491
NM_001128085.1:c.403T>C
CA397682499
NM_001128085.1:c.405T>A
CA397682501
NM_001128085.1:c.405T>G