Canonical Allele Identifier: PA2825641805
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Phe1666Leu
CA10618781
NM_001127511.3:c.4996T>C
CA16032379
NM_001127511.3:c.4998T>A
CA16032380
NM_001127511.3:c.4998T>G