Canonical Allele Identifier: PA2828015258
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 217920
ClinVar RCV Id: RCV000202029 RCV000466853 RCV000571880 RCV000657057 RCV003534474 RCV003997040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala314Thr
CA026910
NM_001354903.2:c.940G>A