Canonical Allele Identifier: PA2827947114
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gln2376His
CA047019
NM_001354895.2:c.7128G>C
CA16036857
NM_001354895.2:c.7128G>T