Canonical Allele Identifier: PA1139729195
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 809507
ClinVar RCV Id: RCV000998101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.Ser512del
CA915942981
NM_001354604.2:c.1534_1536del