Canonical Allele Identifier: PA132234
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43170
ClinVar RCV Id: RCV000036074 RCV000289903 RCV000320261 RCV000384251 RCV000968680 RCV001272499 RCV002504882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Val679Ile
CA132233
NM_000260.4:c.2035G>A