Canonical Allele Identifier: PA2828029044
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala2301Ser
CA16038165
NM_001354906.2:c.6901G>T