Canonical Allele Identifier: PA2828013119
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827296
ClinVar RCV Id: RCV001026888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2463Ser
CA16038427
NM_001354905.2:c.7387A>T