Canonical Allele Identifier: PA188052
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184169
ClinVar RCV Id: RCV000163348 RCV000231340 RCV000758732 RCV000764565 RCV002267901 RCV003153439 RCV003995246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1702Glu
CA009865
NM_001127510.3:c.5105G>A