Canonical Allele Identifier: PA2827962629
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303
ClinVar RCV Id: RCV001026899 RCV003537435
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2636Ser
CA16038447
NM_001354897.2:c.7906A>T
CA16038449
NM_001354897.2:c.7907C>G