Canonical Allele Identifier: PA2825629688
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1799369
ClinVar RCV Id: RCV002444216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Glu1020Asp
CA16028035
NM_001127510.3:c.3060A>C
CA16028036
NM_001127510.3:c.3060A>T