Canonical Allele Identifier: PA2828010891
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro2079Ser
CA16035571
NM_001354902.2:c.6235C>T