Canonical Allele Identifier: PA2825643905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2341Ala
CA046787
NM_001127511.3:c.7021T>G