Canonical Allele Identifier: PA2827961635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2115874
ClinVar RCV Id: RCV003744952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2332Glu
CA16036519
NM_001354897.2:c.6994C>G