Canonical Allele Identifier: PA2825018117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2092648
ClinVar RCV Id: RCV003744871
ClinVar Variation Id: 2683854
ClinVar RCV Id: RCV003484463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn1012Lys
CA16027973
NM_000038.6:c.3036T>A
CA16027974
NM_000038.6:c.3036T>G