Canonical Allele Identifier: PA915981018
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 229003
ClinVar RCV Id: RCV000222966 RCV001276692 RCV001112773 RCV001112774 RCV001112775 RCV000901706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg836Cys
CA6197855
NM_001127180.2:c.2506C>T