Canonical Allele Identifier: PA2828320470
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1505979
ClinVar RCV Id: RCV001999654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Thr1007Ser
CA381944208
NM_001369365.1:c.3019A>T
CA381944210
NM_001369365.1:c.3020C>G