Canonical Allele Identifier: PA645375559
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 241465
ClinVar RCV Id: RCV000233207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Cys25del
CA10583428
NM_024306.5:c.75_77del