Canonical Allele Identifier: PA2827881799
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2113344
ClinVar RCV Id: RCV003027274
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Pro504Ser
CA16040406
NM_001354605.2:c.1510C>T