Canonical Allele Identifier: PA2828046992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gln2250His
CA047019
NM_001354904.2:c.6750G>C
CA16036857
NM_001354904.2:c.6750G>T