Canonical Allele Identifier: PA2825021393
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_000029.2:p.Thr1709Ser
CA16032532
NM_000038.6:c.5125A>T
CA16032534
NM_000038.6:c.5126C>G