Canonical Allele Identifier: PA2827951107
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1055767
ClinVar RCV Id: RCV003169834 RCV003771103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1138Arg
CA16028689
NM_001354896.2:c.3412G>A
CA16028690
NM_001354896.2:c.3412G>C