Canonical Allele Identifier: PA658659878
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469951
ClinVar RCV Id: RCV000532247 RCV000611032 RCV000573595 RCV002231976 RCV002508225 RCV003403314 RCV003999390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln1367Arg
CA16030311
NM_001127510.3:c.4100A>G