Canonical Allele Identifier: PA916039771
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188223
ClinVar RCV Id: RCV000218100 RCV000484713 RCV002291585 RCV003995610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser765Leu
CA007315
NM_001354896.2:c.2294C>T