Canonical Allele Identifier: PA916041659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216183
ClinVar RCV Id: RCV000202229 RCV000572076 RCV000766698 RCV002500621 RCV002515464 RCV003534471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2691Gly
CA049665
NM_001354896.2:c.8071A>G