Canonical Allele Identifier: PA2830431569
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2113344
ClinVar RCV Id: RCV003027274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Pro392Ser
CA16040406
NM_198158.3:c.1174C>T