Canonical Allele Identifier: PA2828022471
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3072801
ClinVar RCV Id: RCV004013823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Pro1301Thr
CA16031747
NM_001354906.2:c.3901C>A