Canonical Allele Identifier: PA2827962547
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069385
ClinVar RCV Id: RCV004007929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2610Arg
CA16038270
NM_001354897.2:c.7829A>G