Canonical Allele Identifier: PA095567
Gene: SART3 HGNC NCBI

Linked Data

ClinVar Variation Id: 849
ClinVar RCV Id: RCV000000897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055521.1:p.Val591Met
CA114574
NM_014706.4:c.1771G>A