Canonical Allele Identifier: PA916041951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411398
ClinVar Variation Id: 485101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His454Gln
CA027188
NM_001354897.2:c.1362T>G
CA16024222
NM_001354897.2:c.1362T>A