Canonical Allele Identifier: PA2826151522
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1197613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Thr405Asn
CA2490655
NM_001184967.2:c.1214C>A