Canonical Allele Identifier: PA132376
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43274
ClinVar RCV Id: RCV000036179 RCV000271936 RCV000367756 RCV000677322 RCV000755320 RCV001273508 RCV002496553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Tyr1719Cys
CA132375
NM_000260.4:c.5156A>G