Canonical Allele Identifier: PA2826151599
Gene: MITF HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171897.1:p.Tyr10Asn
CA353560217
NM_001184968.2:c.28T>A