ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139720258
Gene: SH2D1A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001091714
RCV001327374
ClinVar Variation:
871639
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002342.1:p.Arg55Gln
CA414123516
NM_002351.5:c.164G>A