Canonical Allele Identifier: PA2827967939
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1434Ser
CA038928
NM_001354898.2:c.4301C>G
CA16030912
NM_001354898.2:c.4300A>T