ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825629772
Gene: SMARCAL1
HGNC
NCBI
Linked Data
ClinVar Variation Id:
197797
ClinVar RCV Id:
RCV000178929
RCV001080195
RCV003907622
RCV004020134
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001120679.1:p.Gly321Asp
CA246129
NM_001127207.2:c.962G>A