Canonical Allele Identifier: PA2828011388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 809784
ClinVar RCV Id: RCV001025977 RCV000998416 RCV003744686 RCV004004457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr2193Ser
CA16036710
NM_001354905.2:c.6577A>T
CA16036712
NM_001354905.2:c.6578C>G