Canonical Allele Identifier: PA2827989053
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485159
ClinVar RCV Id: RCV000563660 RCV001153052 RCV000695048 RCV003744570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2289Phe
CA16036569
NM_001354900.2:c.6866C>T