Allele Registry

Canonical Allele Identifier: PA3057321778

Gene: MN1 HGNC NCBI

ClinVar RCV:

RCV004724020

ClinVar Variation:

3343667

HGVS (amino-acid)	Matching Registered Transcripts
NP_002421.3:p.Phe1315Leu	CA411032751 NM_002430.3:c.3945C>G CA411032752 NM_002430.3:c.3945C>A CA411032764 NM_002430.3:c.3943T>C