Canonical Allele Identifier: PA2827976057
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469921
ClinVar RCV Id: RCV000571619 RCV001800755 RCV003651969 RCV003999383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Tyr1115Cys
CA16028846
NM_001354899.2:c.3344A>G