Canonical Allele Identifier: PA2827960409
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1477212
ClinVar RCV Id: RCV003773118
ClinVar Variation Id: 2452715
ClinVar RCV Id: RCV003177489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1958Glu
CA16034112
NM_001354897.2:c.5874T>A
CA16034113
NM_001354897.2:c.5874T>G