Canonical Allele Identifier: PA2829651562
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2947582
ClinVar RCV Id: RCV003804212
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Ser508Arg
CA77003532
NM_006722.2:c.1524C>G
CA353560052
NM_006722.2:c.1522A>C
CA353560058
NM_006722.2:c.1524C>A