Canonical Allele Identifier: PA2827954302
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1469021
ClinVar RCV Id: RCV003773042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg31Ser
CA360611949
NM_001354897.2:c.93G>C
CA360611950
NM_001354897.2:c.93G>T