Canonical Allele Identifier: PA166669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749
ClinVar RCV Id: RCV000119206 RCV000130570 RCV000235422 RCV000677781 RCV001354303 RCV000368182 RCV000588540 RCV003315710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1125Ala
CA008333
NM_000038.6:c.3374T>C