Canonical Allele Identifier: PA2828015626
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_001341835.1:p.Gly204Glu
CA16024504
NM_001354906.2:c.611G>A
CA658683406
NM_001354906.2:c.609_611delinsCGA