Canonical Allele Identifier: PA2573257410
Gene: MYLIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1598643
ClinVar RCV Id: RCV002122681
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Amino-acid Alleles

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