Canonical Allele Identifier: PA2827995983
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 850938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Phe1625Ser
CA16032377
NM_001354901.2:c.4874T>C