Canonical Allele Identifier: PA915981096
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43196
ClinVar RCV Id: RCV000036100 RCV000414534 RCV001580451 RCV003114213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Glu968Asp
CA278647
NM_001127180.2:c.2904G>T
CA381943396
NM_001127180.2:c.2904G>C