Canonical Allele Identifier: PA645462213
Gene: SLX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 407931
ClinVar RCV Id: RCV000474038 RCV000996183 RCV001336769 RCV001194853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115820.2:p.Ile1421Phe
CA7865700
NM_032444.4:c.4261A>T