Canonical Allele Identifier: PA915963484
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334181
ClinVar RCV Id: RCV000347148 RCV000391309 RCV001672571 RCV001837880 RCV000771089 RCV002356463 RCV001094710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr194Met
CA062512
NM_000384.3:c.581C>T