Canonical Allele Identifier: PA916040278
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521
ClinVar RCV Id: RCV000130087 RCV000228695 RCV000590777 RCV003997547 RCV003534377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1511Met
CA009574
NM_001354896.2:c.4532C>T