Canonical Allele Identifier: PA2825105663
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1975262
ClinVar RCV Id: RCV002755585
ClinVar Variation Id: 2580780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Asn323Lys
CA353559531
NM_000248.4:c.969C>A
CA353559532
NM_000248.4:c.969C>G