Canonical Allele Identifier: PA2827971325
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482396
ClinVar RCV Id: RCV000569767 RCV003537148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2466Ile
CA16037587
NM_001354898.2:c.7398G>A
CA16037588
NM_001354898.2:c.7398G>C
CA16037589
NM_001354898.2:c.7398G>T