Canonical Allele Identifier: PA2825641912
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1698Ser
CA040767
NM_001127511.3:c.5093A>G