Canonical Allele Identifier: PA2828007452
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745303
ClinVar RCV Id: RCV002351472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Glu1539Asp
CA16032475
NM_001354905.2:c.4617G>C
CA16032476
NM_001354905.2:c.4617G>T