ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827982920
Gene: APC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
490192
ClinVar RCV Id:
RCV000583252
RCV001192944
RCV003767276
RCV004001279
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341829.1:p.Pro382Thr
CA16024197
NM_001354900.2:c.1144C>A