Canonical Allele Identifier: PA2828029291
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 654022
ClinVar RCV Id: RCV003653372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Glu2502Asp
CA16038295
NM_001354903.2:c.7506A>C
CA16038296
NM_001354903.2:c.7506A>T