Canonical Allele Identifier: PA2828320048
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 242392
ClinVar RCV Id: RCV000674391 RCV000763276 RCV001004800 RCV001854837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg646Trp
CA16616838
NM_001369365.1:c.1936C>T