Canonical Allele Identifier: PA2827970936
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2350His
CA16036850
NM_001354898.2:c.7050A>C
CA16036851
NM_001354898.2:c.7050A>T