Canonical Allele Identifier: PA2827945153
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr1773Ile
CA16032962
NM_001354895.2:c.5318C>T