Canonical Allele Identifier: PA1139746986
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 941928
ClinVar RCV Id: RCV001211804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Met1Ile
CA402998575
NM_138924.3:c.3G>T
CA402998577
NM_138924.3:c.3G>C
CA402998580
NM_138924.3:c.3G>A