Canonical Allele Identifier: PA2826151578
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_001171896.1:p.Met459Ile
CA353560072
NM_001184967.2:c.1377G>T
CA353560073
NM_001184967.2:c.1377G>C
CA353560074
NM_001184967.2:c.1377G>A