Canonical Allele Identifier: PA274184
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188957
ClinVar RCV Id: RCV000169332 RCV001054309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg36Cys
CA274183
NM_000030.3:c.106C>T