Canonical Allele Identifier: PA1139739499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949271
ClinVar RCV Id: RCV003650743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1668Tyr
CA16032166
NM_001354896.2:c.5002A>T