Canonical Allele Identifier: PA2828015748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp390Glu
CA16024530
NM_001354903.2:c.1170C>A
CA16024531
NM_001354903.2:c.1170C>G