Canonical Allele Identifier: PA645396587
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 371917
ClinVar RCV Id: RCV000410173 RCV002230742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro41Leu
CA16042079
NM_001127511.3:c.122C>T