Canonical Allele Identifier: PA2825024949
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn2624Asp
CA16038432
NM_000038.6:c.7870A>G