Canonical Allele Identifier: PA2827989152
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1404451
ClinVar RCV Id: RCV003772768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met2323Leu
CA16036773
NM_001354900.2:c.6967A>C
CA16036774
NM_001354900.2:c.6967A>T