Canonical Allele Identifier: PA1139729102
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 995918
ClinVar RCV Id: RCV001290151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.Arg310Gly
CA353561608
NM_001354604.2:c.928A>G