Canonical Allele Identifier: PA174559
Gene: MYRF HGNC NCBI

Linked Data

ClinVar Variation Id: 161665
ClinVar RCV Id: RCV000149201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037411.1:p.Thr410Met
CA174558
NM_013279.4:c.1229C>T