Canonical Allele Identifier: PA916042498
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106
ClinVar RCV Id: RCV000773795 RCV003744643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp973Glu
CA16028782
NM_001354905.2:c.2919T>A
CA16028783
NM_001354905.2:c.2919T>G