Canonical Allele Identifier: PA2573180535
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_001120652.1:p.Thr1018Ser
CA381944208
NM_001127180.2:c.3052A>T
CA381944210
NM_001127180.2:c.3053C>G