Canonical Allele Identifier: PA2828006696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140839
ClinVar RCV Id: RCV000129037 RCV000148367 RCV000236515 RCV000507260 RCV002514708 RCV003650387 RCV003997474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Cys1418Gly
CA009712
NM_001354905.2:c.4252T>G