Canonical Allele Identifier: PA2827999048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2014516
ClinVar RCV Id: RCV003742946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Glu2558Asp
CA16038391
NM_001354901.2:c.7674A>C
CA16038392
NM_001354901.2:c.7674A>T