Canonical Allele Identifier: PA2827881703
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14277
ClinVar RCV Id: RCV000015347 RCV001541066 RCV002513060 RCV003974827 RCV002281708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Ser404Pro
CA123838
NM_001354605.2:c.1210T>C