Canonical Allele Identifier: PA113220
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 30872
ClinVar RCV Id: RCV000023857 RCV000483483 RCV003317044 RCV002513207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Arg154Cys
CA259930
NM_024306.5:c.460C>T