Canonical Allele Identifier: PA2826929917
Gene: SIMC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2618809
ClinVar RCV Id: RCV004359589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295124.1:p.Tyr519His
CA362245506
NM_001308195.2:c.1555T>C