Canonical Allele Identifier: PA2825024825
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2841190
ClinVar RCV Id: RCV003652389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2592Leu
CA16038220
NM_000038.6:c.7774G>C
CA16038221
NM_000038.6:c.7774G>T