Canonical Allele Identifier: PA2827962766
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2676Asn
CA16038702
NM_001354897.2:c.8027T>A