Canonical Allele Identifier: PA2827954377
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062203
ClinVar RCV Id: RCV003745323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala51Val
CA360612179
NM_001354897.2:c.152C>T