Canonical Allele Identifier: PA2825627799
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43299
ClinVar RCV Id: RCV000036204 RCV000671433 RCV001826554 RCV001531119 RCV003389444 RCV004545738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Gly1904Arg
CA132400
NM_001127180.2:c.5710G>A
CA381954092
NM_001127180.2:c.5710G>C