Canonical Allele Identifier: PA2827882060
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2943489
ClinVar RCV Id: RCV003800607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Glu387Asp
CA77003516
NM_001354606.2:c.1161A>T
CA353559308
NM_001354606.2:c.1161A>C