Canonical Allele Identifier: PA2828014622
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062957
ClinVar RCV Id: RCV003771195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met200Leu
CA16022641
NM_001354903.2:c.598A>C
CA16022643
NM_001354903.2:c.598A>T