Canonical Allele Identifier: PA2827971232
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2439Cys
CA16037430
NM_001354898.2:c.7316C>G