Canonical Allele Identifier: PA915964629
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 237740
ClinVar RCV Id: RCV001837772 RCV002466475 RCV003165602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ala4483Val
CA052795
NM_000384.3:c.13448C>T