Canonical Allele Identifier: PA2828031650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 826163
ClinVar RCV Id: RCV001024848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Glu177Val
CA16022663
NM_001354904.2:c.530A>T