Canonical Allele Identifier: PA2825020689
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1534Val
CA16031411
NM_000038.6:c.4601G>T