Canonical Allele Identifier: PA2827970379
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu2183Ala
CA045546
NM_001354898.2:c.6548A>C