Canonical Allele Identifier: PA915981276
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43216
ClinVar RCV Id: RCV000036120 RCV001852744 RCV003230377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly1218Arg
CA132301
NM_001127180.2:c.3652G>A
CA381947149
NM_001127180.2:c.3652G>C