Canonical Allele Identifier: PA2827970940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2351His
CA047019
NM_001354898.2:c.7053G>C
CA16036857
NM_001354898.2:c.7053G>T