Canonical Allele Identifier: PA2828049034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asp2530Glu
CA16038636
NM_001354904.2:c.7590T>A
CA16038637
NM_001354904.2:c.7590T>G