ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825056611
Gene: FAH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2675349
ClinVar RCV Id:
RCV003468078
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000128.1:p.Gly343Glu
CA393621786
NM_000137.4:c.1028G>A