Canonical Allele Identifier: PA916022151
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 302503
ClinVar RCV Id: RCV000285625 RCV000382429 RCV001859795 RCV002338877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304950.1:p.Ser57Arg
CA6289795
NM_001318021.1:c.171C>A
CA382715483
NM_001318021.1:c.171C>G
CA382715497
NM_001318021.1:c.169A>C