Canonical Allele Identifier: PA2830431567
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Ser391Cys
CA353559992
NM_198158.3:c.1172C>G