Canonical Allele Identifier: PA2573165155
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407727
ClinVar RCV Id: RCV001918585 RCV004010843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1448Ser
CA389040018
NM_000257.4:c.4343A>G