Canonical Allele Identifier: PA2828027618
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Met2090Ile
CA16036834
NM_001354906.2:c.6270G>A
CA16036835
NM_001354906.2:c.6270G>C
CA16036836
NM_001354906.2:c.6270G>T