Canonical Allele Identifier: PA915963762
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 265884
ClinVar RCV Id: RCV000256271 RCV003765569 RCV004021038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser1142Leu
CA058814
NM_000384.3:c.3425C>T