Canonical Allele Identifier: PA2828009139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1369536
ClinVar RCV Id: RCV001870683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1494Ala
CA16031754
NM_001354902.2:c.4480A>G