Canonical Allele Identifier: PA2828321658
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2831860
ClinVar RCV Id: RCV003686817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Trp2028Cys
CA381936353
NM_001369365.1:c.6084G>T
CA381936355
NM_001369365.1:c.6084G>C