Canonical Allele Identifier: PA2825025126
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1025683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2669Ser
CA16038723
NM_000038.6:c.8005C>T