Canonical Allele Identifier: PA2828028606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1722138
ClinVar RCV Id: RCV003743932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn2235Lys
CA16037750
NM_001354906.2:c.6705T>A
CA16037751
NM_001354906.2:c.6705T>G