Canonical Allele Identifier: PA645399879
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411458
ClinVar RCV Id: RCV000570866 RCV000600295 RCV003766580 RCV004001950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln1367His
CA037656
NM_001127510.3:c.4101G>C
CA16030313
NM_001127510.3:c.4101G>T