Canonical Allele Identifier: PA2827980733
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 950600
ClinVar RCV Id: RCV003650754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val2533Leu
CA16038012
NM_001354899.2:c.7597G>C
CA16038013
NM_001354899.2:c.7597G>T