Canonical Allele Identifier: PA2825025084
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp2656Glu
CA16038636
NM_000038.6:c.7968T>A
CA16038637
NM_000038.6:c.7968T>G