Canonical Allele Identifier: PA658668833
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 451477
ClinVar RCV Id: RCV001148363 RCV001148364 RCV000523994 RCV003114651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Asn278Ser
CA2490582
NM_000248.4:c.833A>G