Canonical Allele Identifier: PA2827990125
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433679
ClinVar RCV Id: RCV000502714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp2615Tyr
CA16038632
NM_001354900.2:c.7843G>T