Canonical Allele Identifier: PA2827881966
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900358
ClinVar RCV Id: RCV001145485 RCV001145484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.Asn286Lys
CA353561440
NM_001354606.2:c.858C>A
CA353561441
NM_001354606.2:c.858C>G