Canonical Allele Identifier: PA2827996057
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1395242
ClinVar RCV Id: RCV003772714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1646Asn
CA16032510
NM_001354901.2:c.4937C>A