Canonical Allele Identifier: PA2828026955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489485
ClinVar RCV Id: RCV000580325 RCV001584395 RCV002476261 RCV003537234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr2142Ala
CA045904
NM_001354903.2:c.6424A>G