Canonical Allele Identifier: PA915980997
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306176
ClinVar RCV Id: RCV000280481 RCV000335541 RCV000374878 RCV001240935 RCV001833448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Arg804Gln
CA6197838
NM_001127180.2:c.2411G>A