Canonical Allele Identifier: PA916040696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012
ClinVar RCV Id: RCV000567213 RCV001805184 RCV003313099 RCV003999402 RCV003742741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1861Thr
CA16033423
NM_001354896.2:c.5581C>A