Canonical Allele Identifier: PA2825105720
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2576686
ClinVar RCV Id: RCV003322991
ClinVar Variation Id: 2954441
ClinVar RCV Id: RCV003813664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Thr382Ser
CA353559907
NM_000248.4:c.1144A>T
CA353559909
NM_000248.4:c.1145C>G