Canonical Allele Identifier: PA191798
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185391
ClinVar RCV Id: RCV000164801 RCV000198244 RCV000236550 RCV000657054 RCV001155352 RCV003995365 RCV003316030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val686Ile
CA007204
NM_001127511.3:c.2056G>A