Canonical Allele Identifier: PA2827971246
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2443Pro
CA013665
NM_001354898.2:c.7327T>C