Canonical Allele Identifier: PA645415195
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 264607
ClinVar RCV Id: RCV000243487 RCV000553630 RCV001180069 RCV001529540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp545Asn
CA10587778
NM_000257.4:c.1633G>A