Canonical Allele Identifier: PA2827998632
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391
ClinVar RCV Id: RCV001190625 RCV003770144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp2431Val
CA048153
NM_001354901.2:c.7292A>T