ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA102724
Gene: SMARCAL1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
827737
ClinVar RCV Id:
RCV001027621
RCV001269553
RCV001040718
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001120679.1:p.Arg820His
CA2098212
NM_001127207.2:c.2459G>A