Canonical Allele Identifier: PA2573206032
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1469021
ClinVar RCV Id: RCV003773042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg31Ser
CA360611949
NM_001354902.2:c.93G>C
CA360611950
NM_001354902.2:c.93G>T