Canonical Allele Identifier: PA916040245
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1477Ser
CA038928
NM_001354896.2:c.4430C>G
CA16030912
NM_001354896.2:c.4429A>T