Canonical Allele Identifier: PA2741817265
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 2542991
ClinVar RCV Id: RCV004316480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Thr2473Ser
CA345997200
NM_000384.3:c.7418C>G
CA345997202
NM_000384.3:c.7417A>T