Canonical Allele Identifier: PA2828319641
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2274538
ClinVar RCV Id: RCV002813119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.His316Gln
CA381933248
NM_001369365.1:c.948C>A
CA381933249
NM_001369365.1:c.948C>G