Canonical Allele Identifier: PA2827966946
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1135Ala
CA035507
NM_001354898.2:c.3403A>G