ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA286661
Gene: APC
HGNC
NCBI
Linked Data
ClinVar Variation Id:
127314
ClinVar RCV Id:
RCV000115113
RCV000573892
RCV003534343
RCV003997228
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000029.2:p.Ile2231Phe
CA012398
NM_000038.6:c.6691A>T