Canonical Allele Identifier: PA2825203872
Gene: FGA HGNC NCBI

Linked Data

ClinVar Variation Id: 16401
ClinVar RCV Id: RCV000017842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000499.1:p.Arg38Ser
CA358533872
NM_000508.5:c.114G>C
CA358533874
NM_000508.5:c.114G>T