Canonical Allele Identifier: PA2827995511
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 993040
ClinVar RCV Id: RCV001283862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1476Ser
CA16031416
NM_001354901.2:c.4427A>G