Canonical Allele Identifier: PA2827965253
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485113
ClinVar RCV Id: RCV000574995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly611Ser
CA16025485
NM_001354898.2:c.1831G>A