Canonical Allele Identifier: PA2827968732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184169
ClinVar RCV Id: RCV000163348 RCV000231340 RCV000758732 RCV000764565 RCV002267901 RCV003153439 RCV003995246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1677Glu
CA009865
NM_001354898.2:c.5030G>A