Canonical Allele Identifier: PA2827971635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala2559Ser
CA16038165
NM_001354898.2:c.7675G>T