Canonical Allele Identifier: PA2827882719
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2949784
ClinVar RCV Id: RCV003804950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Leu276Pro
CA353561791
NM_001354608.2:c.827T>C