Canonical Allele Identifier: PA2830433369
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.Asn124Lys
CA353561440
NM_198178.3:c.372C>A
CA353561441
NM_198178.3:c.372C>G