Canonical Allele Identifier: PA916042611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513
ClinVar RCV Id: RCV000572880 RCV003537176 RCV004001004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr877Ala
CA035507
NM_001354906.2:c.2629A>G