Canonical Allele Identifier: PA2827986951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489463
ClinVar RCV Id: RCV000579477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1654Ser
CA16032447
NM_001354900.2:c.4962A>C
CA16032448
NM_001354900.2:c.4962A>T