Canonical Allele Identifier: PA2828055661
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_001341834.1:p.Gly960Arg
CA16028689
NM_001354905.2:c.2878G>A
CA16028690
NM_001354905.2:c.2878G>C