Canonical Allele Identifier: PA916047701
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 196240
ClinVar RCV Id: RCV000177023 RCV001278603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Asp2Glu
CA243131
NM_001369365.1:c.6C>A
CA381947551
NM_001369365.1:c.6C>G