Canonical Allele Identifier: PA202836
Gene: MFRP HGNC NCBI

Linked Data

ClinVar Variation Id: 197357
ClinVar RCV Id: RCV000178370 RCV000334278 RCV000877864 RCV001107826 RCV002492783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113621.1:p.Ile119Val
CA017249
NM_031433.4:c.355A>G