Canonical Allele Identifier: PA2825025848
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1410343
ClinVar RCV Id: RCV001940062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Arg19Trp
CA6289907
NM_000039.3:c.55C>T