Canonical Allele Identifier: PA2827990165
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_001341829.1:p.Pro2628Leu
CA16038726
NM_001354900.2:c.7883C>T