Canonical Allele Identifier: PA916041645
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2674Glu
CA16038636
NM_001354896.2:c.8022T>A
CA16038637
NM_001354896.2:c.8022T>G