Canonical Allele Identifier: PA658825378
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 550334
ClinVar RCV Id: RCV000665056 RCV000885301 RCV001584529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Met49Leu
CA2208988
NM_000030.3:c.145A>C
CA351313262
NM_000030.3:c.145A>T