Canonical Allele Identifier: PA2825641702
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232583
ClinVar RCV Id: RCV000222795 RCV003765428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1629Ser
CA10578386
NM_001127511.3:c.4885A>T