Canonical Allele Identifier: PA2828007790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1069Lys
CA008452
NM_001354902.2:c.3206C>A