Canonical Allele Identifier: PA916038013
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14275
ClinVar RCV Id: RCV000015345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341533.1:p.Asn317Lys
CA213179
NM_001354604.2:c.951C>G
CA353561668
NM_001354604.2:c.951C>A