Canonical Allele Identifier: PA2827986922
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Glu1644Asp
CA16032387
NM_001354900.2:c.4932A>C
CA16032388
NM_001354900.2:c.4932A>T