Canonical Allele Identifier: PA2828321507
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43305
ClinVar RCV Id: RCV000036210 RCV000277461 RCV000312785 RCV000369786 RCV000669735 RCV000963284 RCV001831642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Val1907Ile
CA132407
NM_001369365.1:c.5719G>A