Canonical Allele Identifier: PA2825020932
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1595Ser
CA16031815
NM_000038.6:c.4783G>T