Canonical Allele Identifier: PA2826151559
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1319604
ClinVar RCV Id: RCV003237600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Thr438Ala
CA353559941
NM_001184967.2:c.1312A>G