Canonical Allele Identifier: PA2830431089
Gene: MITF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Tyr10Asn
CA353560217
NM_198158.3:c.28T>A