ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA130227
Gene: FGA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
31443
ClinVar RCV:
RCV000030941
RCV000851581
RCV000851971
RCV001509236
RCV002228034
RCV002476987
RCV004532379
ClinVar Variation:
16404
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000499.1:p.Arg35His
CA130224
NM_000508.5:c.104G>A