Canonical Allele Identifier: PA2828320019
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2662469
ClinVar RCV Id: RCV003443964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Cys624Tyr
CA381938561
NM_001369365.1:c.1871G>A