Canonical Allele Identifier: PA123840
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14277
ClinVar RCV Id: RCV000015347 RCV001541066 RCV002513060 RCV003974827 RCV002281708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Ser298Pro
CA123838
NM_000248.4:c.892T>C