Canonical Allele Identifier: PA2827987221
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1035716
ClinVar RCV Id: RCV003169596 RCV003770884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys1729Asn
CA16032941
NM_001354900.2:c.5187G>C
CA16032942
NM_001354900.2:c.5187G>T