Canonical Allele Identifier: PA2828012312
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr2476Ser
CA16038056
NM_001354902.2:c.7426A>T
CA16038058
NM_001354902.2:c.7427C>G