Canonical Allele Identifier: PA2827971871
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433679
ClinVar RCV Id: RCV000502714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp2631Tyr
CA16038632
NM_001354898.2:c.7891G>T