Canonical Allele Identifier: PA2825020323
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411562
ClinVar Variation Id: 941479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln1444His
CA038623
NM_000038.6:c.4332A>C
CA16030825
NM_000038.6:c.4332A>T