Canonical Allele Identifier: PA2827966757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730254
ClinVar RCV Id: RCV002326430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1084Val
CA16028628
NM_001354898.2:c.3251G>T