Canonical Allele Identifier: PA2827962491
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760417
ClinVar RCV Id: RCV002400793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Glu2592Asp
CA16038154
NM_001354897.2:c.7776A>C
CA16038155
NM_001354897.2:c.7776A>T