Canonical Allele Identifier: PA2827998890
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755
ClinVar RCV Id: RCV003177529 RCV003745562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2508Ser
CA16038056
NM_001354901.2:c.7522A>T
CA16038058
NM_001354901.2:c.7523C>G