Canonical Allele Identifier: PA2827966486
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Tyr1006Cys
CA16028105
NM_001354898.2:c.3017A>G