Canonical Allele Identifier: PA891859696
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 571390
ClinVar RCV Id: RCV000692525 RCV001026031 RCV000758740 RCV003420229 RCV003999584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2367Ala
CA046911
NM_001127510.3:c.7099A>G