Canonical Allele Identifier: PA2827951150
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629106
ClinVar RCV Id: RCV000773795 RCV003744643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1151Glu
CA16028782
NM_001354896.2:c.3453T>A
CA16028783
NM_001354896.2:c.3453T>G