Canonical Allele Identifier: PA891859799
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 579380
ClinVar RCV Id: RCV003534706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Trp2547Arg
CA16037921
NM_001127510.3:c.7639T>A
CA16037922
NM_001127510.3:c.7639T>C