Canonical Allele Identifier: PA2828012743
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2407Ser
CA16038056
NM_001354905.2:c.7219A>T
CA16038058
NM_001354905.2:c.7220C>G