Canonical Allele Identifier: PA2827986919
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350413
ClinVar RCV Id: RCV000280740 RCV000985305 RCV001023479 RCV003535689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Phe1643Leu
CA10618781
NM_001354900.2:c.4927T>C
CA16032379
NM_001354900.2:c.4929T>A
CA16032380
NM_001354900.2:c.4929T>G