Canonical Allele Identifier: PA2827980808
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630201
ClinVar RCV Id: RCV000775350 RCV001566386 RCV003653306 RCV004001446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2556Thr
CA049041
NM_001354899.2:c.7666G>A