Canonical Allele Identifier: PA916022136
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17920
ClinVar RCV Id: RCV000019513 RCV001508677 RCV002496420
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Arg34Leu
CA127563
NM_001318018.2:c.101G>T