Canonical Allele Identifier: PA2828029539
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp2373Glu
CA16038636
NM_001354906.2:c.7119T>A
CA16038637
NM_001354906.2:c.7119T>G