Canonical Allele Identifier: PA2580113601
Gene: MAT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1716437
ClinVar RCV Id: RCV002303494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000420.1:p.Met164Ile
CA377362701
NM_000429.3:c.492G>T
CA377362702
NM_000429.3:c.492G>C
CA377362703
NM_000429.3:c.492G>A