Canonical Allele Identifier: PA2827995949
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630006
ClinVar RCV Id: RCV000774872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly1615Ala
CA16032318
NM_001354901.2:c.4844G>C