Canonical Allele Identifier: PA2827999001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069385
ClinVar RCV Id: RCV004007929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln2541Arg
CA16038270
NM_001354901.2:c.7622A>G