Canonical Allele Identifier: PA645397514
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_001120864.1:p.Thr419Met
CA174558
NM_001127392.3:c.1256C>T