Canonical Allele Identifier: PA2827961731
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2362Asn
CA16036703
NM_001354897.2:c.7085G>A