ClinGen Allele Registry
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Canonical Allele Identifier:
PA091328
Gene: AGXT
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
186658
ClinVar RCV:
RCV000169358
RCV001386996
ClinVar Variation:
188979
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000021.1:p.Ser218Leu
CA274210
NM_000030.3:c.653C>T