Canonical Allele Identifier: PA2827998884
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039868
ClinVar RCV Id: RCV002242334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Trp2505Cys
CA16038038
NM_001354901.2:c.7515G>C
CA16038039
NM_001354901.2:c.7515G>T