Canonical Allele Identifier: PA2825634842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2359Ala
CA046787
NM_001127510.3:c.7075T>G