Canonical Allele Identifier: PA2827947888
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957922
ClinVar RCV Id: RCV003650807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly2610Ala
CA16038341
NM_001354895.2:c.7829G>C