Canonical Allele Identifier: PA2825539344
Gene: MYH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401309
ClinVar RCV Id: RCV001906267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093582.1:p.Met360Leu
CA287745464
NM_001100112.2:c.1078A>T
CA398163050
NM_001100112.2:c.1078A>C