Canonical Allele Identifier: PA2825025091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2659Leu
CA16038652
NM_000038.6:c.7975G>C
CA16038653
NM_000038.6:c.7975G>T