Canonical Allele Identifier: PA2825021660
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631456
ClinVar RCV Id: RCV000777890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val1776Leu
CA16032974
NM_000038.6:c.5326G>C
CA16032975
NM_000038.6:c.5326G>T