Canonical Allele Identifier: PA916038028
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14273
ClinVar RCV Id: RCV000015343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.Ser357Pro
CA123830
NM_001354604.2:c.1069T>C