Canonical Allele Identifier: PA2827986141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr1404Ile
CA009453
NM_001354900.2:c.4211C>T