Canonical Allele Identifier: PA2827980776
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 918607
ClinVar RCV Id: RCV001176273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2548Pro
CA16038109
NM_001354899.2:c.7642G>C