Canonical Allele Identifier: PA2825021223
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744737
ClinVar RCV Id: RCV002351378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu1668Asp
CA16032282
NM_000038.6:c.5004G>C
CA16032283
NM_000038.6:c.5004G>T