Canonical Allele Identifier: PA2827982777
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2755578
ClinVar RCV Id: RCV003536840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp338Glu
CA16023913
NM_001354900.2:c.1014C>A
CA16023914
NM_001354900.2:c.1014C>G