Canonical Allele Identifier: PA114554
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822
ClinVar RCV Id: RCV000000864 RCV000000865 RCV000020088 RCV000034388 RCV000120049 RCV000115087 RCV000210085 RCV000238802 RCV000722046 RCV001195214 RCV001554302 RCV001824556 RCV001535784 RCV003650351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1289Lys
CA008761
NM_001127511.3:c.3866T>A