Canonical Allele Identifier: PA2826151474
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Pro350Ala
CA2490626
NM_001184967.2:c.1048C>G