Canonical Allele Identifier: PA916041561
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470107
ClinVar RCV Id: RCV003742796
ClinVar Variation Id: 2773659
ClinVar RCV Id: RCV003585632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp2606Glu
CA049085
NM_001354896.2:c.7818T>G
CA16038196
NM_001354896.2:c.7818T>A