Canonical Allele Identifier: PA2827966877
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411461
ClinVar RCV Id: RCV000561662 RCV001775817 RCV003535732 RCV004001952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1117Thr
CA035313
NM_001354898.2:c.3350A>C