Canonical Allele Identifier: PA2828052136
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1025291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Lys252Asn
CA16023349
NM_001354905.2:c.756G>C
CA16023350
NM_001354905.2:c.756G>T