Canonical Allele Identifier: PA2825644723
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2609Phe
CA049365
NM_001127511.3:c.7826C>T