Canonical Allele Identifier: PA2830433601
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1975262
ClinVar RCV Id: RCV002755585
ClinVar Variation Id: 2580780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.Asn261Lys
CA353559531
NM_198178.3:c.783C>A
CA353559532
NM_198178.3:c.783C>G