Canonical Allele Identifier: PA2828015728
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490205
ClinVar RCV Id: RCV000582681
ClinVar Variation Id: 1018692
ClinVar RCV Id: RCV002241988 RCV002395683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly386Glu
CA16024504
NM_001354903.2:c.1157G>A
CA658683406
NM_001354903.2:c.1155_1157delinsCGA