Canonical Allele Identifier: PA2828023229
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469991
ClinVar RCV Id: RCV001189874 RCV001775866 RCV003742727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr1426Ser
CA16032532
NM_001354906.2:c.4276A>T
CA16032534
NM_001354906.2:c.4277C>G