Canonical Allele Identifier: PA2825636981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062203
ClinVar RCV Id: RCV003745323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala51Val
CA360612179
NM_001127511.3:c.152C>T