Canonical Allele Identifier: PA2828053886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2681902
ClinVar RCV Id: RCV003477194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly475Arg
CA16025480
NM_001354905.2:c.1423G>A
CA16025481
NM_001354905.2:c.1423G>C