Canonical Allele Identifier: PA2827952168
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_001341825.1:p.Glu1686Asp
CA16032282
NM_001354896.2:c.5058G>C
CA16032283
NM_001354896.2:c.5058G>T