Canonical Allele Identifier: PA2580147609
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2088602
ClinVar RCV Id: RCV003011723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Cys453Arg
CA381935219
NM_001127180.2:c.1357T>C