Canonical Allele Identifier: PA915980780
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306167
ClinVar RCV Id: RCV000274537 RCV000329699 RCV000374942 RCV002522208 RCV000940796 RCV001274700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Cys453Tyr
CA6197483
NM_001127180.2:c.1358G>A