Canonical Allele Identifier: PA2828320466
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1402203
ClinVar RCV Id: RCV001925058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Thr1003Met
CA381944184
NM_001369365.1:c.3008C>T