Canonical Allele Identifier: PA2828006553
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2444634
ClinVar RCV Id: RCV003154402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gly1374Arg
CA16031406
NM_001354905.2:c.4120G>A
CA16031407
NM_001354905.2:c.4120G>C