Canonical Allele Identifier: PA2825025068
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 620612
ClinVar RCV Id: RCV000761072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2651Leu
CA16038597
NM_000038.6:c.7951G>C