Canonical Allele Identifier: PA2830433211
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2937538
ClinVar RCV Id: RCV003794168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937820.1:p.Met495Ile
CA353560072
NM_198177.3:c.1485G>T
CA353560073
NM_198177.3:c.1485G>C
CA353560074
NM_198177.3:c.1485G>A