Canonical Allele Identifier: PA2825105745
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2947582
ClinVar RCV Id: RCV003804212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Ser408Arg
CA77003532
NM_000248.4:c.1224C>G
CA353560052
NM_000248.4:c.1222A>C
CA353560058
NM_000248.4:c.1224C>A