Canonical Allele Identifier: PA2827962530
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692385
ClinVar RCV Id: RCV002257179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2604Ala
CA16038234
NM_001354897.2:c.7810T>G