Canonical Allele Identifier: PA2827959464
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655826
ClinVar RCV Id: RCV003536010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu1673Asp
CA16032250
NM_001354897.2:c.5019A>C
CA16032251
NM_001354897.2:c.5019A>T