Canonical Allele Identifier: PA2827946002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp2036Asn
CA16034696
NM_001354895.2:c.6106G>A