Canonical Allele Identifier: PA2827881635
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_001341534.1:p.Leu333Pro
CA353561791
NM_001354605.2:c.998T>C