Canonical Allele Identifier: PA2827986491
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1742135
ClinVar RCV Id: RCV002330441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1507Lys
CA16031507
NM_001354900.2:c.4521C>A
CA16031508
NM_001354900.2:c.4521C>G