Canonical Allele Identifier: PA2828012340
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2337Trp
CA16037624
NM_001354905.2:c.7010C>G