Canonical Allele Identifier: PA645444006
Gene: PAFAH1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436135
ClinVar RCV Id: RCV000500121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000421.1:p.Arg20Ser
CA397637963
NM_000430.4:c.58C>A