Canonical Allele Identifier: PA2825636984
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1061069
ClinVar RCV Id: RCV003652224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser52Arg
CA360612181
NM_001127511.3:c.154A>C
CA360612194
NM_001127511.3:c.156C>A
CA360612197
NM_001127511.3:c.156C>G