Allele Registry

Canonical Allele Identifier: PA2573257410

Gene: MYLIP HGNC NCBI

ClinVar RCV:

RCV002122681

ClinVar Variation:

1598643

HGVS (amino-acid)	Matching Registered Transcripts
NP_037394.2:p.Asn342Ser	CA3644627 NM_013262.4:c.1025A>G