Canonical Allele Identifier: PA916039606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480
ClinVar RCV Id: RCV000144570 RCV000222854 RCV000485323 RCV000766534 RCV003315924 RCV003998159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr580Met
CA005437
NM_001354896.2:c.1739C>T