Canonical Allele Identifier: PA2826976042
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17920
ClinVar RCV Id: RCV000019513 RCV001508677 RCV002496420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Arg34Leu
CA127563
NM_001318017.2:c.101G>T