Canonical Allele Identifier: PA2827978161
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631456
ClinVar RCV Id: RCV000777890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val1748Leu
CA16032974
NM_001354899.2:c.5242G>C
CA16032975
NM_001354899.2:c.5242G>T