Canonical Allele Identifier: PA2827960529
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411389
ClinVar RCV Id: RCV000475886 RCV000573470 RCV003535730 RCV003126748 RCV003479128 RCV004001932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro1996Leu
CA043504
NM_001354897.2:c.5987C>T