Canonical Allele Identifier: PA2828012082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2304Cys
CA16037430
NM_001354905.2:c.6911C>G