Canonical Allele Identifier: PA2825025925
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513939
ClinVar RCV Id: RCV002018517 RCV002498049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Val91Leu
CA382717089
NM_000039.3:c.271G>T
CA382717092
NM_000039.3:c.271G>C