Canonical Allele Identifier: PA658802941
Gene: PAFAH1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 502295
ClinVar RCV Id: RCV000591042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000421.1:p.Asp141Asn
CA397639851
NM_000430.4:c.421G>A