Canonical Allele Identifier: PA2827954012
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841190
ClinVar RCV Id: RCV003652389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val2610Leu
CA16038220
NM_001354896.2:c.7828G>C
CA16038221
NM_001354896.2:c.7828G>T