Canonical Allele Identifier: PA916041142
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41510
ClinVar RCV Id: RCV000034395 RCV000115114 RCV000211930 RCV000515374 RCV000664301 RCV000987580 RCV001151801 RCV001353961 RCV003944874 RCV003534318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2260Gly
CA012449
NM_001354896.2:c.6778A>G