Canonical Allele Identifier: PA2828004783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2819088
ClinVar RCV Id: RCV003650881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser47Ala
CA360612124
NM_001354902.2:c.139T>G