Canonical Allele Identifier: PA127557
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17915
ClinVar RCV Id: RCV000019504 RCV001851952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Pro28Arg
CA127555
NM_000039.3:c.83C>G