Canonical Allele Identifier: PA2828009719
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 847431
ClinVar RCV Id: RCV002240216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1682Ala
CA16032958
NM_001354902.2:c.5044A>G