Canonical Allele Identifier: PA2825636334
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1364164
ClinVar RCV Id: RCV003745362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Tyr1642Cys
CA040224
NM_001127510.3:c.4925A>G