Canonical Allele Identifier: PA2827971627
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 964392
ClinVar RCV Id: RCV003652079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu2557Lys
CA16038148
NM_001354898.2:c.7669G>A