Canonical Allele Identifier: PA2828029096
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841190
ClinVar RCV Id: RCV003652389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val2309Leu
CA16038220
NM_001354906.2:c.6925G>C
CA16038221
NM_001354906.2:c.6925G>T