Canonical Allele Identifier: PA2827981659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135728
ClinVar RCV Id: RCV000122813 RCV001017958 RCV003997392 RCV003415925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2814Ala
CA015593
NM_001354899.2:c.8440T>G