Canonical Allele Identifier: PA2827962747
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761476
ClinVar RCV Id: RCV002419056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2671Met
CA16038668
NM_001354897.2:c.8013T>G