Canonical Allele Identifier: PA2827996022
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 638969
ClinVar RCV Id: RCV003653322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser1637Gly
CA16032450
NM_001354901.2:c.4909A>G