Canonical Allele Identifier: PA2828007477
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156
ClinVar RCV Id: RCV000573523 RCV003767216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1540Thr
CA16032477
NM_001354905.2:c.4618G>A