Canonical Allele Identifier: PA2828001993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly1221Ala
CA008783
NM_001354902.2:c.3662G>C