Canonical Allele Identifier: PA2830431228
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2663180
ClinVar RCV Id: RCV003442368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Gln161His
CA77001739
NM_198158.3:c.483A>T
CA353561328
NM_198158.3:c.483A>C