Canonical Allele Identifier: PA915980850
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 11856
ClinVar RCV Id: RCV000012631 RCV000012630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Met599Ile
CA121721
NM_001127180.2:c.1797G>A
CA381937289
NM_001127180.2:c.1797G>T
CA381937291
NM_001127180.2:c.1797G>C