Canonical Allele Identifier: PA2828003961
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411542
ClinVar RCV Id: RCV003651892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Leu2310Val
CA16037014
NM_001354902.2:c.6928C>G