Canonical Allele Identifier: PA2825186366
Gene: AMT HGNC NCBI

Linked Data

ClinVar Variation Id: 645153
ClinVar RCV Id: RCV000799186
ClinVar Variation Id: 971783
ClinVar RCV Id: RCV001247646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000472.2:p.Val50Leu
CA2398464
NM_000481.4:c.148G>T
CA2398465
NM_000481.4:c.148G>C