Canonical Allele Identifier: PA2825105694
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1305242
ClinVar RCV Id: RCV001768449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Gly357Val
CA353559748
NM_000248.4:c.1070G>T