Canonical Allele Identifier: PA2827955109
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104
ClinVar RCV Id: RCV001026715 RCV000985321 RCV003742794 RCV003999432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp266Glu
CA16023011
NM_001354897.2:c.798T>A
CA16023012
NM_001354897.2:c.798T>G