Canonical Allele Identifier: PA2827987217
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1374809
ClinVar RCV Id: RCV003745371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys1727Asn
CA16032926
NM_001354900.2:c.5181G>C
CA16032927
NM_001354900.2:c.5181G>T