Canonical Allele Identifier: PA2827995282
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419
ClinVar RCV Id: RCV000471930 RCV000565410 RCV002260641 RCV003316572 RCV002481466 RCV004001941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1408Ser
CA038968
NM_001354901.2:c.4222C>T