Canonical Allele Identifier: PA2828320630
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438177
ClinVar RCV Id: RCV000505067 RCV000670174 RCV001047383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Asn1171Lys
CA381946913
NM_001369365.1:c.3513C>A
CA381946914
NM_001369365.1:c.3513C>G