Canonical Allele Identifier: PA2825635091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp2490Val
CA048153
NM_001127510.3:c.7469A>T