Canonical Allele Identifier: PA916041292
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_001341825.1:p.Thr2371Ser
CA16036710
NM_001354896.2:c.7111A>T
CA16036712
NM_001354896.2:c.7112C>G