Canonical Allele Identifier: PA915980622
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43264
ClinVar RCV Id: RCV000036169 RCV000434773 RCV000666360 RCV001826551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Thr165Met
CA278676
NM_001127180.2:c.494C>T