Canonical Allele Identifier: PA2825503974
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040630
ClinVar RCV Id: RCV001344306 RCV003169660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Met971Val
CA374111821
NM_001083604.3:c.2911A>G