Canonical Allele Identifier: PA2741867457
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2947582
ClinVar RCV Id: RCV003804212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.Ser515Arg
CA77003532
NM_001354604.2:c.1545C>G
CA353560052
NM_001354604.2:c.1543A>C
CA353560058
NM_001354604.2:c.1545C>A