Canonical Allele Identifier: PA2741991040
Gene: MFRP HGNC NCBI

Linked Data

ClinVar Variation Id: 2607031
ClinVar RCV Id: RCV003355062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113621.1:p.Arg527Cys
CA6320059
NM_031433.4:c.1579C>T