Canonical Allele Identifier: PA2827971575
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2542Ser
CA16038056
NM_001354898.2:c.7624A>T
CA16038058
NM_001354898.2:c.7625C>G