Canonical Allele Identifier: PA2825635332
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp2656Glu
CA16038636
NM_001127510.3:c.7968T>A
CA16038637
NM_001127510.3:c.7968T>G