Canonical Allele Identifier: PA2827989662
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567031
ClinVar RCV Id: RCV003278300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2474Leu
CA16037724
NM_001354900.2:c.7420A>C
CA16037725
NM_001354900.2:c.7420A>T