Canonical Allele Identifier: PA2827962757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2673Gly
CA16038681
NM_001354897.2:c.8018A>G