Canonical Allele Identifier: PA2825635194
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1009233
ClinVar RCV Id: RCV003770591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu2558Phe
CA16037997
NM_001127510.3:c.7672C>T