Canonical Allele Identifier: PA2827955682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490205
ClinVar RCV Id: RCV000582681
ClinVar Variation Id: 1018692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gly497Glu
CA16024504
NM_001354897.2:c.1490G>A
CA658683406
NM_001354897.2:c.1488_1490delinsCGA