Canonical Allele Identifier: PA658660701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482240
ClinVar RCV Id: RCV000564293 RCV000985320 RCV002526839 RCV003537098 RCV004000939
ClinVar Variation Id: 642835
ClinVar RCV Id: RCV002268286 RCV001026543 RCV003535879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2514Ser
CA048379
NM_001127510.3:c.7541C>G
CA16037721
NM_001127510.3:c.7540A>T