Canonical Allele Identifier: PA2827961734
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 809784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2363Ser
CA16036710
NM_001354897.2:c.7087A>T
CA16036712
NM_001354897.2:c.7088C>G