Canonical Allele Identifier: PA645375624
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 320500
ClinVar RCV Id: RCV000342958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Pro129Ser
CA10638356
NM_024306.5:c.385C>T