Canonical Allele Identifier: PA2827962080
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489494
ClinVar RCV Id: RCV000579671 RCV003156263 RCV003767267 RCV004001233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala2470Pro
CA047824
NM_001354897.2:c.7408G>C