Canonical Allele Identifier: PA2827973676
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2755578
ClinVar RCV Id: RCV003536840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp369Glu
CA16023913
NM_001354899.2:c.1107C>A
CA16023914
NM_001354899.2:c.1107C>G