Canonical Allele Identifier: PA1139741836
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927393
ClinVar RCV Id: RCV001190628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu2576Val
CA048920
NM_001354896.2:c.7726C>G