Canonical Allele Identifier: PA127565
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_000030.1:p.Arg34Leu
CA127563
NM_000039.3:c.101G>T