Canonical Allele Identifier: PA2825025082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 495374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp2656Gly
CA16038634
NM_000038.6:c.7967A>G