ClinGen Allele Registry
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Canonical Allele Identifier:
PA346670
Gene: SNTA1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000157504
RCV000413113
RCV000529567
RCV000621647
ClinVar Variation:
180527
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003089.1:p.Arg197Trp
CA346668
NM_003098.3:c.589C>T