Canonical Allele Identifier: PA2827962507
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470107
ClinVar RCV Id: RCV003742796
ClinVar Variation Id: 2773659
ClinVar RCV Id: RCV003585632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2598Glu
CA049085
NM_001354897.2:c.7794T>G
CA16038196
NM_001354897.2:c.7794T>A