Canonical Allele Identifier: PA2827980327
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537519
ClinVar RCV Id: RCV003538489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2412His
CA16037271
NM_001354899.2:c.7236G>C
CA16037272
NM_001354899.2:c.7236G>T