Canonical Allele Identifier: PA2827971763
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827303
ClinVar RCV Id: RCV001026899 RCV003537435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr2601Ser
CA16038447
NM_001354898.2:c.7801A>T
CA16038449
NM_001354898.2:c.7802C>G