Canonical Allele Identifier: PA2825644338
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924012
ClinVar RCV Id: RCV001185127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2480Pro
CA16037626
NM_001127511.3:c.7438T>C