Canonical Allele Identifier: PA916040608
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631456
ClinVar RCV Id: RCV000777890
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val1794Leu
CA16032974
NM_001354896.2:c.5380G>C
CA16032975
NM_001354896.2:c.5380G>T