Canonical Allele Identifier: PA2827989189
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1359860
ClinVar RCV Id: RCV003772508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln2334Pro
CA16036847
NM_001354900.2:c.7001A>C