Canonical Allele Identifier: PA2827970881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2331Ala
CA046771
NM_001354898.2:c.6991A>G