Canonical Allele Identifier: PA915980778
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438678
ClinVar RCV Id: RCV000505567 RCV001229028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Glu450Val
CA381935201
NM_001127180.2:c.1349A>T