Canonical Allele Identifier: PA2827882881
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Ser446Cys
CA353559992
NM_001354608.2:c.1337C>G