Canonical Allele Identifier: PA2825644838
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1376108
ClinVar RCV Id: RCV003534764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asp2645Tyr
CA16038679
NM_001127511.3:c.7933G>T