Canonical Allele Identifier: PA2827999036
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2861029
ClinVar RCV Id: RCV003743178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Trp2553Ser
CA16038351
NM_001354901.2:c.7658G>C