Canonical Allele Identifier: PA2827960401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350415
ClinVar Variation Id: 3230807
ClinVar RCV Id: RCV004522921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1957Ser
CA043197
NM_001354897.2:c.5870C>G
CA16034103
NM_001354897.2:c.5869A>T