Canonical Allele Identifier: PA2499289992
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 989137
ClinVar RCV Id: RCV001391535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Gly64Trp
CA396768226
NM_024306.5:c.190G>T