Canonical Allele Identifier: PA2827882095
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_001341535.1:p.Asn423Lys
CA353559531
NM_001354606.2:c.1269C>A
CA353559532
NM_001354606.2:c.1269C>G