Canonical Allele Identifier: PA2827995238
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127295
ClinVar RCV Id: RCV000115092 RCV000148365 RCV000200964 RCV000238996 RCV000264340 RCV000586737 RCV001270348 RCV000987572 RCV003650370
ClinVar Variation Id: 3001945
ClinVar RCV Id: RCV003863008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys1395Glu
CA009483
NM_001354901.2:c.4183A>G
CA2740094004
NM_001354901.2:c.4182_4183delinsCG