Canonical Allele Identifier: PA891859844
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 584680
ClinVar RCV Id: RCV000708975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2675Ser
CA16038758
NM_001127510.3:c.8023C>T