Canonical Allele Identifier: PA2827882893
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2937538
ClinVar RCV Id: RCV003794168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Met459Ile
CA353560072
NM_001354608.2:c.1377G>T
CA353560073
NM_001354608.2:c.1377G>C
CA353560074
NM_001354608.2:c.1377G>A