Canonical Allele Identifier: PA2825644861
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1721928
ClinVar RCV Id: RCV003743928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2651Leu
CA16038726
NM_001127511.3:c.7952C>T