Canonical Allele Identifier: PA2828015007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2755578
ClinVar RCV Id: RCV003536840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asp114Glu
CA16023913
NM_001354906.2:c.342C>A
CA16023914
NM_001354906.2:c.342C>G