Canonical Allele Identifier: PA2825056445
Gene: FAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1896364
ClinVar RCV Id: RCV002575145 RCV004064320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000128.1:p.Met177Val
CA393619904
NM_000137.4:c.529A>G