Canonical Allele Identifier: PA2827996236
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 864178
ClinVar RCV Id: RCV003650594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1697Ala
CA16032845
NM_001354901.2:c.5089T>G
CA916079919
NM_001354901.2:c.5088_5091delinsTGCG