Canonical Allele Identifier: PA2828011913
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537519
ClinVar RCV Id: RCV003538489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln2280His
CA16037271
NM_001354905.2:c.6840G>C
CA16037272
NM_001354905.2:c.6840G>T