Canonical Allele Identifier: PA1139765190
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.Asn287Lys
CA353561440
NM_198159.3:c.861C>A
CA353561441
NM_198159.3:c.861C>G