Canonical Allele Identifier: PA2827974079
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537485
ClinVar RCV Id: RCV001012236 RCV002268233 RCV002530050 RCV003538466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gly496Asp
CA028449
NM_001354899.2:c.1487G>A