Canonical Allele Identifier: PA916040698
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127306
ClinVar RCV Id: RCV000115104 RCV000202997 RCV000148372 RCV000572635 RCV000679068 RCV003315229 RCV003650372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1861Leu
CA010490
NM_001354896.2:c.5582C>T