Canonical Allele Identifier: PA2828045901
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro2044Ser
CA16035571
NM_001354904.2:c.6130C>T