Canonical Allele Identifier: PA098620
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43012
ClinVar RCV Id: RCV000035906 RCV000162336 RCV000148704 RCV000177508 RCV000247619 RCV000466190 RCV000656145 RCV000758029 RCV001109803 RCV001270174 RCV002504881 RCV003320077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1459Asn
CA014901
NM_000257.4:c.4377G>T
CA389038810
NM_000257.4:c.4377G>C