Canonical Allele Identifier: PA658810043
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 506003
ClinVar RCV Id: RCV000604068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.Ala395Val
CA353559351
NM_198159.3:c.1184C>T