Canonical Allele Identifier: PA2828027633
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln2093His
CA047019
NM_001354906.2:c.6279G>C
CA16036857
NM_001354906.2:c.6279G>T