Canonical Allele Identifier: PA2827998216
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1404451
ClinVar RCV Id: RCV003772768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met2305Leu
CA16036773
NM_001354901.2:c.6913A>C
CA16036774
NM_001354901.2:c.6913A>T