ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826581687
Gene: ENG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
213212
ClinVar RCV Id:
RCV000229345
RCV000791433
RCV000755259
RCV002399723
RCV003907720
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001265067.1:p.Arg347His
CA321073
NM_001278138.2:c.1040G>A