Canonical Allele Identifier: PA2827995257
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1400Ser
CA038928
NM_001354901.2:c.4199C>G
CA16030912
NM_001354901.2:c.4198A>T