Canonical Allele Identifier: PA2825025128
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1721928
ClinVar RCV Id: RCV003743928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2669Leu
CA16038726
NM_000038.6:c.8006C>T