Canonical Allele Identifier: PA645375767
Gene: FA2H HGNC NCBI

Linked Data

ClinVar Variation Id: 320492
ClinVar RCV Id: RCV000262979 RCV000863033 RCV002056508 RCV001848662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077282.3:p.Thr363Pro
CA8170305
NM_024306.5:c.1087A>C