Canonical Allele Identifier: PA2827968735
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133532
ClinVar RCV Id: RCV000120042 RCV000562439 RCV000663189 RCV001582590 RCV003534354 RCV003997333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1678Ala
CA009873
NM_001354898.2:c.5033G>C