Canonical Allele Identifier: PA915964625
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 630236
ClinVar RCV Id: RCV003166055 RCV003106053 RCV003327459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Gln4474His
CA052673
NM_000384.3:c.13422G>C
CA345967443
NM_000384.3:c.13422G>T