Canonical Allele Identifier: PA2825029078
Gene: ASPA HGNC NCBI

Linked Data

ClinVar Variation Id: 844740
ClinVar RCV Id: RCV001047671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000040.1:p.Leu247Pro
CA397686383
NM_000049.4:c.740T>C