Canonical Allele Identifier: PA2828004397
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg2579Ile
CA16038731
NM_001354902.2:c.7736G>T