Canonical Allele Identifier: PA2827990182
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069608
ClinVar RCV Id: RCV004008152 RCV004371939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg2632Ser
CA16038748
NM_001354900.2:c.7896A>C
CA16038749
NM_001354900.2:c.7896A>T