Canonical Allele Identifier: PA2827987155
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln1711Glu
CA16032822
NM_001354900.2:c.5131C>G