Canonical Allele Identifier: PA2573169004
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1392676
ClinVar RCV Id: RCV001882238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Tyr271Cys
CA377360841
NM_000429.3:c.812A>G