Canonical Allele Identifier: PA2827990123
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2615Glu
CA16038636
NM_001354900.2:c.7845T>A
CA16038637
NM_001354900.2:c.7845T>G