Canonical Allele Identifier: PA658660822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112
ClinVar RCV Id: RCV000572911 RCV002527879 RCV001558793 RCV003742799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2611Lys
CA049276
NM_001127510.3:c.7832C>A