ClinGen Allele Registry
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Canonical Allele Identifier:
PA916062866
Gene: VSX1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000005560
RCV000358879
RCV000454465
RCV002054416
ClinVar Variation:
5248
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_955457.1:p.Gly160Asp
CA117355
NM_199425.3:c.479G>A