Canonical Allele Identifier: PA2573166282
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1515132
ClinVar RCV Id: RCV002020863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys234Asn
CA389052224
NM_000257.4:c.702G>T
CA389052225
NM_000257.4:c.702G>C