Canonical Allele Identifier: PA2828003456
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp1988Ala
CA044147
NM_001354902.2:c.5963A>C