Canonical Allele Identifier: PA658659700
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_001120982.1:p.Tyr1143Cys
CA16028846
NM_001127510.3:c.3428A>G