Canonical Allele Identifier: PA166116
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141681
ClinVar RCV Id: RCV000130294 RCV000255155 RCV000410458 RCV001192912 RCV003998052 RCV003534379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2261Leu
CA012518
NM_001127510.3:c.6782C>T