Canonical Allele Identifier: PA2827957612
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1118Ser
CA035035
NM_001354897.2:c.3353A>G