Canonical Allele Identifier: PA2825015979
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624846
ClinVar RCV Id: RCV003387067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile638Thr
CA16025499
NM_000038.6:c.1913T>C