Canonical Allele Identifier: PA2573165071
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1409624
ClinVar RCV Id: RCV001913814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys876Asn
CA389047954
NM_000257.4:c.2628G>T
CA389047955
NM_000257.4:c.2628G>C