Canonical Allele Identifier: PA645400223
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1716Ser
CA040767
NM_001127510.3:c.5147A>G