Canonical Allele Identifier: PA2827971568
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039868
ClinVar RCV Id: RCV002242334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Trp2539Cys
CA16038038
NM_001354898.2:c.7617G>C
CA16038039
NM_001354898.2:c.7617G>T