Canonical Allele Identifier: PA353553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 224553
ClinVar RCV Id: RCV000562346 RCV003743640 RCV000210203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Tyr1027Cys
CA353549
NM_000038.6:c.3080A>G