Canonical Allele Identifier: PA2828016561
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714967
ClinVar RCV Id: RCV003743845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr527Ser
CA16025436
NM_001354903.2:c.1579A>T
CA16025438
NM_001354903.2:c.1580C>G