Canonical Allele Identifier: PA2827952137
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_001341825.1:p.Cys1661Ser
CA16032121
NM_001354896.2:c.4981T>A
CA16032124
NM_001354896.2:c.4982G>C