Canonical Allele Identifier: PA2825025457
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2107310
ClinVar RCV Id: RCV003744920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2748Leu
CA16039217
NM_000038.6:c.8242G>C
CA16039218
NM_000038.6:c.8242G>T