Canonical Allele Identifier: PA2825025380
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2730Ser
CA16039107
NM_000038.6:c.8188G>T