Canonical Allele Identifier: PA2828004383
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp2572Gly
CA16038681
NM_001354902.2:c.7715A>G