Canonical Allele Identifier: PA16040107
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln2376His
CA047019
NM_000038.6:c.7128G>C
CA16036857
NM_000038.6:c.7128G>T