Canonical Allele Identifier: PA2828049100
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg2544Gly
CA16038727
NM_001354904.2:c.7630A>G