Canonical Allele Identifier: PA2825105729
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1722868
ClinVar RCV Id: RCV002305975 RCV003098033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Pro391Leu
CA353559958
NM_000248.4:c.1172C>T