Canonical Allele Identifier: PA2573205681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1404451
ClinVar RCV Id: RCV003772768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Met2382Leu
CA16036773
NM_001354896.2:c.7144A>C
CA16036774
NM_001354896.2:c.7144A>T