Canonical Allele Identifier: PA2825643955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln2358His
CA047019
NM_001127511.3:c.7074G>C
CA16036857
NM_001127511.3:c.7074G>T