Canonical Allele Identifier: PA2827971539
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2530Ala
CA16037981
NM_001354898.2:c.7588T>G