ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825629786
Gene: SMARCAL1
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000342892
RCV000765601
ClinVar Variation:
281779
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001120679.1:p.Arg334Gln
CA2097754
NM_001127207.2:c.1001G>A