Canonical Allele Identifier: PA2825628209
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438179
ClinVar RCV Id: RCV000504907 RCV001857218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Thr2144Met
CA381938356
NM_001127180.2:c.6431C>T