Canonical Allele Identifier: PA645505849
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 389591
ClinVar RCV Id: RCV000440703 RCV004022448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000255.2:p.Ile385Val
CA16605583
NM_000264.5:c.1153A>G