Canonical Allele Identifier: PA2828019039
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727545
ClinVar RCV Id: RCV002325885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp750Glu
CA034409
NM_001354906.2:c.2250T>A
CA16028121
NM_001354906.2:c.2250T>G