Canonical Allele Identifier: PA2825025155
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg2673Ser
CA16038748
NM_000038.6:c.8019A>C
CA16038749
NM_000038.6:c.8019A>T