Canonical Allele Identifier: PA915964037
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 334128
ClinVar RCV Id: RCV000336043 RCV000372264 RCV002374574 RCV001837853 RCV004544622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000375.3:p.Glu2414Asp
CA064235
NM_000384.3:c.7242A>C
CA064242
NM_000384.3:c.7242A>T