Canonical Allele Identifier: PA915964575
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 128418
ClinVar RCV Id: RCV000116382 RCV000256262 RCV001094749 RCV000845573 RCV000284555 RCV001811403 RCV001837453 RCV000771025 RCV002381422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Ser4338Asn
CA022788
NM_000384.3:c.13013G>A