Canonical Allele Identifier: PA645475954
Gene: MFRP HGNC NCBI

Linked Data

ClinVar Variation Id: 302965
ClinVar RCV Id: RCV000288629 RCV000383217 RCV001104328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113621.1:p.His262Gln
CA6320391
NM_031433.4:c.786T>A
CA382976900
NM_031433.4:c.786T>G