Canonical Allele Identifier: PA127542
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17910
ClinVar RCV Id: RCV000019499 RCV002513123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Pro167Arg
CA127540
NM_000039.3:c.500C>G