Canonical Allele Identifier: PA2828029014
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009233
ClinVar RCV Id: RCV003770591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu2457Phe
CA16037997
NM_001354903.2:c.7369C>T