Canonical Allele Identifier: PA2828051879
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1764696
ClinVar RCV Id: RCV002373690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser234Arg
CA16023234
NM_001354905.2:c.700A>C
CA16023240
NM_001354905.2:c.702T>A
CA16023241
NM_001354905.2:c.702T>G