Canonical Allele Identifier: PA2827971914
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1721928
ClinVar RCV Id: RCV003743928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2644Leu
CA16038726
NM_001354898.2:c.7931C>T