Canonical Allele Identifier: PA2573290657
Gene: MFRP HGNC NCBI

Linked Data

ClinVar Variation Id: 1378813
ClinVar RCV Id: RCV001914696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113621.1:p.Leu535Pro
CA382971551
NM_031433.4:c.1604T>C