Canonical Allele Identifier: PA2499233649
Gene: WRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1003302
ClinVar RCV Id: RCV001299835
ClinVar Variation Id: 1418730
ClinVar RCV Id: RCV001952258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000544.2:p.Met1130Leu
CA4705052
NM_000553.6:c.3388A>T
CA370925148
NM_000553.6:c.3388A>C