Canonical Allele Identifier: PA2827989932
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039177
ClinVar RCV Id: RCV003770925 RCV004036000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2557Ser
CA16038256
NM_001354900.2:c.7669A>T
CA16038257
NM_001354900.2:c.7670C>G