Canonical Allele Identifier: PA2828019698
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1017Ser
CA16028677
NM_001354903.2:c.3050A>G