Canonical Allele Identifier: PA2828022856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2080400
ClinVar RCV Id: RCV003744845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Cys1360Ser
CA16032121
NM_001354906.2:c.4078T>A
CA16032124
NM_001354906.2:c.4079G>C