Canonical Allele Identifier: PA2827966822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 559963
ClinVar RCV Id: RCV000677776
ClinVar Variation Id: 573701
ClinVar RCV Id: RCV003534639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln1102His
CA16028741
NM_001354898.2:c.3306G>C
CA16028742
NM_001354898.2:c.3306G>T