ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825630321
Gene: SMARCAL1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2203262
ClinVar RCV Id:
RCV002651605
RCV003236952
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001120679.1:p.Arg817Cys
CA350504710
NM_001127207.2:c.2449C>T