Canonical Allele Identifier: PA2828027800
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gln2275His
CA047019
NM_001354903.2:c.6825G>C
CA16036857
NM_001354903.2:c.6825G>T