Canonical Allele Identifier: PA2827947808
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ala2584Ser
CA16038165
NM_001354895.2:c.7750G>T