Canonical Allele Identifier: PA2827994262
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1101Ala
CA035507
NM_001354901.2:c.3301A>G