Canonical Allele Identifier: PA2827947041
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2352Gly
CA16036702
NM_001354895.2:c.7054A>G