Canonical Allele Identifier: PA2825644541
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2549Ser
CA16038056
NM_001127511.3:c.7645A>T
CA16038058
NM_001127511.3:c.7646C>G