Canonical Allele Identifier: PA2827980464
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939283
ClinVar RCV Id: RCV003398936 RCV004010669 RCV003538608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr2453Ser
CA16037526
NM_001354899.2:c.7357A>T
CA16037528
NM_001354899.2:c.7358C>G